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L-adenosine is a high-purity adenosine deaminase (ADA) inhibitor provided as a powdered research reagent for in vitro biochemical and cellular studies. The 25 mg vial is suitable for assay development, enzymatic assays, and dose-response experiments, with documented solubility and recommended storage conditions to preserve stability.
High purity (99.82%).
Suitable for in vitro biochemical and cellular assays.
Powdered solid supplied as a 25 mg vial for small-scale studies.
Soluble in DMSO (~8.33 mg/mL) with ultrasonic assistance; hygroscopic solvent may affect solubility.
Store at 4°C protected from light; in solvent: -80°C up to 6 months or -20°C up to 1 month.
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Cytarabine triphosphate trisodium is the trisodium salt of cytarabine's active triphosphate metabolite, provided as a concentrated aqueous solution for biochemical and molecular biology research focused on DNA synthesis and nucleoside metabolism.
Supplied as a 5 mg solution at 100 mM (100 μL) in water.
Active metabolite that inhibits DNA synthesis, suitable for assay and mechanistic studies.
Liquid formulation, colorless to light yellow, for direct use in experiments.
Store at -20°C; solution stability reported up to 2 years.
Chemical formula C9H13N3Na3O14P3 and molecular weight approximately 549.1 g/mol.
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Adenosine (CAS 58-61-7) is a purine nucleoside consisting of adenine covalently linked to a ribose sugar via a -N9-glycosidic bond Endogenously adenosine modulates cellular signaling through activation of specific G protein-coupled adenosine receptors (A1 A2A A2B and A3) influencing diverse physiological processes such as neurotransmission vasodilation and immune responses In biomedical research adenosine is widely utilized to investigate purinergic signaling pathways cardiac function and the regulation of inflammatory and neuroprotective mechanisms as well as serving as a pharmacological tool in receptor binding and functional assays
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LDE225 Diphosphate (CAS 1218778-77-8) is a highly potent and selective antagonist of the Smoothened (Smo) receptor a seven-transmembrane protein involved in the Hedgehog (Hh) signaling pathway LDE225 inhibits Smo with IC50 values of 1 3 nM for murine and 2 5 nM for human Smo resulting in suppression of Hh signaling This pathway is implicated in cellular differentiation proliferation and oncogenesis In vitro LDE225 selectively binds Smo inhibiting Hh-dependent tumor cell growth In vivo it demonstrates dose-dependent antitumor efficacy in medulloblastoma xenograft mouse models LDE225 continues to be explored as a research tool and therapeutic candidate in Hh pathway-driven malignancies
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Adenosine A1 receptor activator T62 is a selective positive allosteric modulator of the adenosine A1 receptor supplied for in vitro research. It is available as a solid or as a ready-to-use 10 mM solution in DMSO, with reported purity of 98.93% and a molecular weight of 291.80 g/mol. Follow the SDS for storage and safe handling.
Allosteric enhancer of adenosine A1 receptor.
Available as solid or 10 mM solution in DMSO.
High reported purity suitable for biochemical and cellular assays.
High solubility in DMSO (100 mg/mL) for easy formulation.
Multilingual SDS provided for safety and handling guidance.
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